Unlock instant, AI-driven research and patent intelligence for your innovation.

Application of supramolecular framework materials based on eight-membered melon rings in drug controlled release

An eight-membered melon ring and frame material technology, which can be used in drug combinations, medical preparations with non-active ingredients, and medical preparations containing active ingredients, etc.

Active Publication Date: 2021-08-24
GUIZHOU UNIV
View PDF3 Cites 0 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

There are many substances currently used for drug sustained release, but there is no report on the use of eight-membered cucurbit rings for the sustained release of drug molecules.

Method used

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
View more

Image

Smart Image Click on the blue labels to locate them in the text.
Viewing Examples
Smart Image
  • Application of supramolecular framework materials based on eight-membered melon rings in drug controlled release
  • Application of supramolecular framework materials based on eight-membered melon rings in drug controlled release
  • Application of supramolecular framework materials based on eight-membered melon rings in drug controlled release

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0049] Example 1: The application of a supramolecular framework material based on eight-membered melon rings in drug controlled release is to dissolve the eight-membered melon rings in a hydrochloric acid solution with a concentration of 6mol / L, and dissolve 5g per liter of hydrochloric acid solution Eight-membered melon rings, left to stand for 7 days to obtain colorless crystals, after filtration, the crystals were dried in a vacuum oven, which was the supramolecular framework material of eight-membered melon rings; adefovir was dissolved in water to make a concentration of 1×10 -3 For the aqueous solution of M, add 1 g of the supramolecular framework material of eight-membered cucurbit rings to every 4 ml of aqueous solution, shake in a water bath at room temperature for 2 hours to load drug molecules, filter and dry, and obtain the supramolecular framework materials of eight-membered cucurbit rings loaded with adefovir.

Embodiment 2

[0050] Example 2: The application of a supramolecular framework material based on eight-membered melon rings in the controlled release of drugs is to dissolve the eight-membered melon rings in a hydrochloric acid solution with a concentration of 6mol / L, and dissolve 3g per liter of hydrochloric acid solution The eight-membered melon ring was left to stand for 5 days to obtain colorless crystals. After filtering, the crystal was dried in a vacuum oven to form the supramolecular framework material of the eight-membered melon ring; levofloxacin was dissolved in water to make a concentration of 1×10 -3 For the aqueous solution of M, add 0.5 g of the supramolecular framework material of eight-membered cucurbit rings to every 4 ml of aqueous solution, shake in a water bath at room temperature for 1 hour to load drug molecules, filter and dry to obtain the supramolecular framework materials of eight-membered cucurbit rings loaded with levofloxacin.

Embodiment 3

[0051] Example 3: The application of a supramolecular framework material based on eight-membered melon rings in the controlled release of drugs is to dissolve the eight-membered melon rings in hydrochloric acid solution with a concentration of 6mol / L, and dissolve 7g per liter of hydrochloric acid solution The eight-membered melon ring was left to stand for 10 days to obtain colorless crystals, and after filtration, the crystal was dried in a vacuum oven to become the supramolecular framework material of the eight-membered melon ring; the didanosin was dissolved in water to make a concentration of 1×10 -3 For the aqueous solution of M, add 1.5 g of supramolecular framework material of eight-membered melon ring to every 4 ml of aqueous solution, shake in a water bath at room temperature for 3 hours to load drug molecules, filter and dry to obtain supramolecular framework material of eight-membered melon ring loaded with didanosin .

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

PUM

No PUM Login to View More

Abstract

The invention discloses an application of a supramolecular frame material based on eight-membered melon rings in drug controlled and sustained release. Drug molecules are loaded on the supramolecular frame material based on eight-membered melon rings, and the slow release of drug molecules is achieved through acid response stimulation. . The invention is a new application of the eight-membered melon ring, which has the characteristics of realizing the sustained release of drug molecules in the human body; in addition, it can also be used as a carrier for drug molecule transport.

Description

technical field [0001] The invention relates to the application of a supramolecular framework material based on eight-membered cucurbit ring, in particular to the application of the supramolecular framework material based on eight-membered cucurbit ring in drug controlled release. Background technique [0002] Cucurbit[n]uril, also known as cucurbit[n]uril, (abbreviated as CB[n] or Q[n]), named for its structure resembling pumpkin, is a macrocycle following crown ether, cyclodextrin and calixarene. Another new type of cage-like host compound after the compound. From the perspective of structural properties, the cucurbit ring has a highly symmetrical hydrophobic cavity and open and full of polar carbonyl oxygen atoms. The above characteristics of this structure make It can selectively include small molecules such as organic, inorganic and biomolecules of appropriate size in the solution state, or have a hydrophilic coordination with dipole or ionic compounds at the port. With...

Claims

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

Application Information

Patent Timeline
no application Login to View More
Patent Type & Authority Patents(China)
IPC IPC(8): A61K47/69A61K31/708A61K31/7068A61K31/675A61K31/5383A61P31/20A61P31/22A61P31/04A61P31/18A61P35/00
CPCA61K31/5383A61K31/675A61K31/7068A61K31/708A61K47/6949A61P31/04A61P31/18A61P31/20A61P31/22A61P35/00
Inventor 肖昕冯华明罗阳刘明陶朱
Owner GUIZHOU UNIV